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Title: Genetics and molecular biology of hydrogen metabolism in sulfate reducing bacteria

Technical Report ·
DOI:https://doi.org/10.2172/6892389· OSTI ID:6892389

The work proposed to be accomplished in the previous funding period was to develop a procedure for genetic exchange based on conjugation mediated by broad host-range plasmids. Such a system has recently been identified that employs IncQ group plasmids and a Desulfovibrio desulfuricans G100A derivative as recipient. During the search for conjugation, we also identified a defective bacteriophage capable of generalized transduction of fragments of chromosomal DNA between mutants of Desulfovibrio desulfuricans. Some of the factors influencing the production and transduction by this defective phage have been investigated. A curious observation was made concerning the response of colonies of these sulfate-reducing bacteria upon exposure to air. All the cells of a colony do not die. Some survive, most likely by producing sulfide at a rate sufficient to provide an anaerobic environment. Dramatic colony morphological changes occur and these have been documented by scanning and transmission electron microscopy. Finally a small endogenous plasmid has been isolated from Desulfovibrio desulfuricans G100A. It has been stably subcloned into a sequencing vector, and nested deletions of this plasmid are being prepared. This plasmid may be useful for the development of a shuttle cloning vector that could be used in more diverse Desulfovibrio. Many of the techniques now to be used in the mutant analysis of hydrogenase genes in the sulfate-reducing bacteria have been successfully applied in an analysis of hydrogenase functions of Rhodobacter capsulatus. 8 figs., 2 tabs.

Research Organization:
Missouri Univ., Columbia, MO (USA). Dept. of Biochemistry
Sponsoring Organization:
DOE/ER
DOE Contract Number:
FG02-87ER13713
OSTI ID:
6892389
Report Number(s):
DOE/ER/13713-4; ON: DE90012692
Country of Publication:
United States
Language:
English